Direct M Fresh S.A. de C.V.
FDA import alert and refusal historySanta Catarina, Mexico
Recorded by FDA as DIRECT M FRESH S.A. DE C.V.; Direct M. Fresh SA de CV
As of October 26, 2026, Direct M Fresh S.A. de C.V. (Santa Catarina, Mexico) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for pikechi mango with chili and lime, published by FDA on August 8, 2018, is also listed on Import Alert 45-02 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-21 · red listIA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Direct M Fresh S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 99-21red listPikechi Mango With Chili And LimeSource
2013
- Import alert listingListed on Import Alert 45-02red listPikechi Mango With Chili And Lime; Dehydrated Mango Strips with chili and lemon; Pikechi Mango With Chili And Lime; Direct Hibiscus Flower JamaicaSource
Questions about Direct M Fresh S.A. de C.V.
- Is Direct M Fresh S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Direct M Fresh S.A. de C.V. is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for pikechi mango with chili and lime; FDA published the listing on August 8, 2018.
- Has FDA refused shipments from Direct M Fresh S.A. de C.V.?
- No FDA import refusals for Direct M Fresh S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- Can shipments from Direct M Fresh S.A. de C.V. still enter the U.S.?
- Shipments of pikechi mango with chili and lime from Direct M Fresh S.A. de C.V. can be detained without physical examination under Import Alert 99-21; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.